Canonical Allele Identifier: PA2829299811
Gene: VIPAS39 HGNC NCBI

Linked Data

ClinVar Variation Id: 2629356
ClinVar RCV Id: RCV003412159

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387256.1:p.Ala243Val
CA263810239
NM_001400327.1:c.728C>T